126,26 €
140,29 €
-10% with code: EXTRA
Pharmacovigilance Medical Writing
126,26 € 
- We will send in 10–14 business days.
Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e.g. scheduling, source data, department/functions involved in document preparation/review, appropria…
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- Author: Justina Orleans-Lindsay
- Publisher: Wiley-Blackwell
- ISBN-10: 1119967260
- ISBN-13: 9781119967262
- Format: 13.7 x 21.3 x 1.3 cm, softcover
- Language: English
- SAVE -10% with code: EXTRA
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Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e.g. scheduling, source data, department/functions involved in document preparation/review, appropriate timelines and planning activities), ending with a generic model document compliant with the current guidelines, which can be modified to meet specific company and product requirements.EXTRA 10 % discount with code: EXTRA
126,26 €
140,29 €
We will send in 10–14 business days.
The promotion ends in 17d.14:01:08
The discount code is valid when purchasing from 10 €. Discounts do not stack.
- Author: Justina Orleans-Lindsay
- Publisher: Wiley-Blackwell
- ISBN-10: 1119967260
- ISBN-13: 9781119967262
- Format: 13.7 x 21.3 x 1.3 cm, softcover
- Language: English English
Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e.g. scheduling, source data, department/functions involved in document preparation/review, appropriate timelines and planning activities), ending with a generic model document compliant with the current guidelines, which can be modified to meet specific company and product requirements.
Reviews